Inactivated vaccine-elicited potent antibodies can broadly neutralize SARS-CoV-2 circulating variants

病毒学 单克隆抗体 抗体 中和 接种疫苗 多克隆抗体 灭活疫苗 生物 效力 中和抗体 疫苗效力 免疫学 病毒 体外 遗传学
作者
Yubin Liu,Ziyi Wang,Xinyu Zhuang,Shengnan Zhang,Zhicheng Chen,Yan Zou,Jie Sheng,Tianpeng Li,Wanbo Tai,Jinfang Yu,Yanqun Wang,Zhaoyong Zhang,Yunfeng Chen,Liangqin Tong,Xi Yu,Linjuan Wu,Dong Chen,Renli Zhang,Ningyi Jin,Weijun Shen
出处
期刊:Nature Communications [Nature Portfolio]
卷期号:14 (1) 被引量:33
标识
DOI:10.1038/s41467-023-37926-7
摘要

A full understanding of the inactivated COVID-19 vaccine-mediated antibody responses to SARS-CoV-2 circulating variants will inform vaccine effectiveness and vaccination development strategies. Here, we offer insights into the inactivated vaccine-induced antibody responses after prime-boost vaccination at both the polyclonal and monoclonal levels. We characterized the VDJ sequence of 118 monoclonal antibodies (mAbs) and found that 20 neutralizing mAbs showed varied potency and breadth against a range of variants including XBB.1.5, BQ.1.1, and BN.1. Bispecific antibodies (bsAbs) based on nonoverlapping mAbs exhibited enhanced neutralizing potency and breadth against the most antibody-evasive strains, such as XBB.1.5, BQ.1.1, and BN.1. The passive transfer of mAbs or their bsAb effectively protected female hACE2 transgenic mice from challenge with an infectious Delta or Omicron BA.2 variant. The neutralization mechanisms of these antibodies were determined by structural characterization. Overall, a broad spectrum of potent and distinct neutralizing antibodies can be induced in individuals immunized with the SARS-CoV-2 inactivated vaccine BBIBP-CorV, suggesting the application potential of inactivated vaccines and these antibodies for preventing infection by SARS-CoV-2 circulating variants.
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